Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP430286.RAhKagRkScT879sY0LLA1dJaFfX6gsyZ6h_kgX5uVQ3yM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP430286.RAhKagRkScT879sY0LLA1dJaFfX6gsyZ6h_kgX5uVQ3yM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP430286.RAhKagRkScT879sY0LLA1dJaFfX6gsyZ6h_kgX5uVQ3yM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP430286.RAhKagRkScT879sY0LLA1dJaFfX6gsyZ6h_kgX5uVQ3yM130_provenance.
- NP430286.RAhKagRkScT879sY0LLA1dJaFfX6gsyZ6h_kgX5uVQ3yM130_assertion description "[In this study, we have tested nine patients with a CMPD or MDS/MPD and a translocation involving 5q31-33 for disruption of PDGFRB by two-colour fluorescence in situ hybridization (FISH) using differentially labelled, closely flanking probes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP430286.RAhKagRkScT879sY0LLA1dJaFfX6gsyZ6h_kgX5uVQ3yM130_provenance.
- NP430286.RAhKagRkScT879sY0LLA1dJaFfX6gsyZ6h_kgX5uVQ3yM130_assertion evidence source_evidence_literature NP430286.RAhKagRkScT879sY0LLA1dJaFfX6gsyZ6h_kgX5uVQ3yM130_provenance.
- NP430286.RAhKagRkScT879sY0LLA1dJaFfX6gsyZ6h_kgX5uVQ3yM130_assertion SIO_000772 12542482 NP430286.RAhKagRkScT879sY0LLA1dJaFfX6gsyZ6h_kgX5uVQ3yM130_provenance.
- NP430286.RAhKagRkScT879sY0LLA1dJaFfX6gsyZ6h_kgX5uVQ3yM130_assertion wasDerivedFrom befree-20140225 NP430286.RAhKagRkScT879sY0LLA1dJaFfX6gsyZ6h_kgX5uVQ3yM130_provenance.
- NP430286.RAhKagRkScT879sY0LLA1dJaFfX6gsyZ6h_kgX5uVQ3yM130_assertion wasGeneratedBy ECO_0000203 NP430286.RAhKagRkScT879sY0LLA1dJaFfX6gsyZ6h_kgX5uVQ3yM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP430286.RAhKagRkScT879sY0LLA1dJaFfX6gsyZ6h_kgX5uVQ3yM130_provenance.